Pharmacovigilance III
Workshop
Pharmaceutical companies are required to collect and enter all adverse drug reactions reports in data bases and to report them to the competent authorities. A significant part of these adverse drug reactions must be evaluated before. The core of this workshop lies in single case evaluation. Through many practical examples and exercises you will learn step by step to write a competent evaluation.
Target audience
This workshop is aimed at everyone who needs to work with single case evaluations.
Date
23.02.2012, Berlin
14.06.2012, Berlin
27.09.2012, Berlin
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